Abstract
| - Three compounds, [Cu(4,4‘-bpy)]2MoO4·2H2O (1), [Cu(4,4‘-bpy)]2Mo2O7 (2), and [Cu(4,4‘-bpy)(nic)(H2O)]2Mo8O26 (3), are synthesized by hydrothermal reaction, which suggests thatoxomolybdate−organic ligand coordination transition-metal fragments can merge their meritto generate some interesting architectures. Crystal data for [Cu(4,4‘-bpy)]2MoO4·2H2O (1): monoclinic system, space group C2/c, a = 10.936(1), b = 17.775(1), and c = 14.484(1) Å, β =110.15(1)°, and Z = 4. Crystal data for [Cu(4,4‘-bpy)]2Mo2O7 (2): orthorhombic system, spacegroup Pbcn, a = 11.841(1), b = 9.105(1), and c = 21.311(1) Å, and Z = 4. Crystal data for[Cu(4,4‘-bpy)(nic)(H2O)]2Mo8O26 (3): monoclinic system, space group P2(1)/n, a = 11.457(1),b = 16.918(1), and c = 12.463(1) Å, β = 92.6(1)°, and Z = 2. Compound 1 is built up from{MoO4} tetrahedra linking of 4,4‘-bpy coordination copper(I) chain fragments as a railroad-like framework. Compound 2 has noticeable structural features: two {Mo2O7} and four{CuO2N2} tetrahedra are connected to each other alternately in a pattern of corner sharingto construct an eight-metal-central-membered cavity; such subunits are connected to eachother also through corner-shared, two-dimensional mosaic frameworks, which are linkedfurther by bidentate 4,4‘-bpy ligands to a three-dimensional framework with oval channels.The two-dimensional flat brick wall-like layer structure of 3 is constructed from two layer[Cu(4,4‘-bpy)(nic)(H2O)]n2n+ chains joined together by β-[Mo8O26]4- units as tethers throughcovalent bonding of the terminal oxo groups to form rectangular cavities. The most curiousfeature of 3, however, is that the extended structure of 3 is comprised of an interpenetratedarrangement of two kinds of multizigzag chain polymers entangled together. The successfulassembly of the three polymeric frameworks of 1−3 demonstrates the dramatic influence ofthe reaction acidity/basicity on the organization of molecular building groups and furtheron the construction of solid architectures. The studies of the temperature dependence of themagnetic susceptibilities of 3 reveal that there exists the weak magnetic transformation of4,4‘-bpy and octamolybdate between metal ions.
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